Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP851616.RAuTCHiLC5yfGTGuZnUhLbqvI2ffjFsaXymfZ0AwyTWRk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP851616.RAuTCHiLC5yfGTGuZnUhLbqvI2ffjFsaXymfZ0AwyTWRk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP851616.RAuTCHiLC5yfGTGuZnUhLbqvI2ffjFsaXymfZ0AwyTWRk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP851616.RAuTCHiLC5yfGTGuZnUhLbqvI2ffjFsaXymfZ0AwyTWRk130_provenance.
- NP851616.RAuTCHiLC5yfGTGuZnUhLbqvI2ffjFsaXymfZ0AwyTWRk130_assertion description "[Like the adult form of the disorder, JHD is a hereditary neurodegenerative disease characterized by dementia and behavioral changes, caused by an expanded CAG repeat within the first exon of the huntingtin (HTT) gene on chromosome 4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP851616.RAuTCHiLC5yfGTGuZnUhLbqvI2ffjFsaXymfZ0AwyTWRk130_provenance.
- NP851616.RAuTCHiLC5yfGTGuZnUhLbqvI2ffjFsaXymfZ0AwyTWRk130_assertion evidence source_evidence_literature NP851616.RAuTCHiLC5yfGTGuZnUhLbqvI2ffjFsaXymfZ0AwyTWRk130_provenance.
- NP851616.RAuTCHiLC5yfGTGuZnUhLbqvI2ffjFsaXymfZ0AwyTWRk130_assertion SIO_000772 23390171 NP851616.RAuTCHiLC5yfGTGuZnUhLbqvI2ffjFsaXymfZ0AwyTWRk130_provenance.
- NP851616.RAuTCHiLC5yfGTGuZnUhLbqvI2ffjFsaXymfZ0AwyTWRk130_assertion wasDerivedFrom befree-20140225 NP851616.RAuTCHiLC5yfGTGuZnUhLbqvI2ffjFsaXymfZ0AwyTWRk130_provenance.
- NP851616.RAuTCHiLC5yfGTGuZnUhLbqvI2ffjFsaXymfZ0AwyTWRk130_assertion wasGeneratedBy ECO_0000203 NP851616.RAuTCHiLC5yfGTGuZnUhLbqvI2ffjFsaXymfZ0AwyTWRk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP851616.RAuTCHiLC5yfGTGuZnUhLbqvI2ffjFsaXymfZ0AwyTWRk130_provenance.